Canonical Allele Identifier: PA2579931489
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2821352
ClinVar RCV Id: RCV003628010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gln165Lys
CA378921150
NM_001130442.3:c.493C>A