Canonical Allele Identifier: PA2829601163
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2820359
ClinVar RCV Id: RCV003627985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Asn172Lys
CA378921078
NM_005343.4:c.516C>A
CA378921080
NM_005343.4:c.516C>G