Canonical Allele Identifier: PA2825692561
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1011612
ClinVar RCV Id: RCV001309436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Val187Ala
CA378920872
NM_001130442.3:c.560T>C