Canonical Allele Identifier: PA2579932378
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1938886
ClinVar RCV Id: RCV002646576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Val160Gly
CA378921172
NM_001130442.3:c.479T>G