Canonical Allele Identifier: PA2573070217
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1334241
ClinVar RCV Id: RCV001813656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Pro95His
CA378921056
NM_001318054.2:c.284C>A