Canonical Allele Identifier: PA2826977558
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Met103Ile
CA5779209
NM_001318054.2:c.309G>A
CA378920945
NM_001318054.2:c.309G>T
CA378920946
NM_001318054.2:c.309G>C