Allele Registry

Canonical Allele Identifier: PA2830359835

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000013445

RCV000419902

RCV000426668

RCV000427529

RCV000436017

RCV000436710

RCV000444744

ClinVar Variation:

12611

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Ala146Val	CA256494 NM_176795.5:c.437C>T