Canonical Allele Identifier: PA296058
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40436
ClinVar RCV Id: RCV000157917 RCV001387769
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly60Asp
CA296057
NM_005343.4:c.179G>A