Canonical Allele Identifier: PA2579932821
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1060724
ClinVar RCV Id: RCV001370190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Tyr71His
CA378924610
NM_001130442.3:c.211T>C