Allele Registry

Canonical Allele Identifier: PA2830359842

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV002885723

RCV003395528

ClinVar Variation:

2037387

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Arg149Gln	CA378922726 NM_176795.5:c.446G>A