Canonical Allele Identifier: PA2825692529
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 724759
ClinVar RCV Id: RCV000898724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Pro179Ala
CA378920995
NM_001130442.3:c.535C>G