Allele Registry

Canonical Allele Identifier: PA645475423

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000229010

RCV003993902

ClinVar Variation:

240138

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