Allele Registry

Canonical Allele Identifier: PA2580532841

Gene: HRAS HGNC NCBI

ClinVar Allele:

2064605

ClinVar RCV:

RCV002846474

ClinVar Variation:

2015677

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Lys88Glu	CA378924414 NM_176795.5:c.262A>G