ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA160027
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0516009566
Score
-0.1013104824
Score
0.0246883304
Score
0.0062915285
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000121201
RCV000813562
ClinVar Variation:
134514
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Thr158Met
CA160026
NM_005343.4:c.473C>T