ClinGen Allele Registry
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Canonical Allele Identifier:
PA129949
Gene: HRAS
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013447
RCV000029211
RCV000032851
RCV000149829
RCV000212495
RCV000418395
RCV000419553
RCV000421701
RCV000422023
RCV000424087
RCV000424380
RCV000426992
RCV000427213
RCV000428012
RCV000429096
RCV000429404
RCV000431602
RCV000431815
RCV000434677
RCV000436505
RCV000436802
RCV000437868
RCV000438707
RCV000438902
RCV000439243
RCV000440052
RCV000443678
RCV000443826
RCV000444512
RCV000445233
RCV000762849
ClinVar Variation:
12613
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Gly12Cys
CA129948
NM_005343.4:c.34G>T