Allele Registry

Canonical Allele Identifier: PA2826977558

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000229010

RCV003993902

ClinVar Variation:

240138

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