Canonical Allele Identifier: PA2826977552
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 948441
ClinVar RCV Id: RCV001219695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Gly101Asp
CA378920975
NM_001318054.2:c.302G>A