Canonical Allele Identifier: PA2825692552
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Met182Val
CA296070
NM_001130442.3:c.544A>G