Canonical Allele Identifier: PA2829600915
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 665374
ClinVar RCV Id: RCV000823640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Asp92Ala
CA378924344
NM_005343.4:c.275A>C