ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA273159
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0105702034
Score
0.2677074837
Score
-0.1696813932
Score
0
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000150836
RCV000255809
ClinVar Variation:
163690
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Gly12Glu
CA273158
NM_005343.4:c.35_36delinsAA