Canonical Allele Identifier: PA2829601139
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2098197
ClinVar RCV Id: RCV003030820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu162Asp
CA378921160
NM_005343.4:c.486G>C
CA378921161
NM_005343.4:c.486G>T