Allele Registry

Canonical Allele Identifier: PA2825692547

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000229010

RCV003993902

ClinVar Variation:

240138

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Met182Ile	CA5779209 NM_001130442.3:c.546G>A CA378920945 NM_001130442.3:c.546G>T CA378920946 NM_001130442.3:c.546G>C