Canonical Allele Identifier: PA2579932738
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1008068
ClinVar RCV Id: RCV001305343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Tyr157His
CA378921197
NM_001130442.3:c.469T>C