Canonical Allele Identifier: PA2829601117
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2146977
ClinVar RCV Id: RCV003076952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr158Arg
CA378921185
NM_005343.4:c.473C>G