Allele Registry

Canonical Allele Identifier: PA2830359837

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000417704

RCV000418346

RCV000427905

RCV000429488

RCV000439018

RCV000439704

ClinVar Variation:

376442

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Ala146Pro	CA16602877 NM_176795.5:c.436G>C