Canonical Allele Identifier: PA645475423
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Met182Ile
CA5779209
NM_005343.4:c.546G>A
CA378920945
NM_005343.4:c.546G>T
CA378920946
NM_005343.4:c.546G>C