Canonical Allele Identifier: PA2579932008
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1321132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Val152Met
CA378921257
NM_001130442.3:c.454G>A