Canonical Allele Identifier: PA2829600891
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1008810
ClinVar RCV Id: RCV001306208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Phe82Ser
CA378924503
NM_005343.4:c.245T>C