Allele Registry

Canonical Allele Identifier: PA2829601083

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.2431703568

Score -0.0292968822

Score 0.4382661473

Score 0.1056014108

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417704

RCV000418346

RCV000427905

RCV000429488

RCV000439018

RCV000439704

ClinVar Variation:

376442

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Ala146Pro	CA16602877 NM_005343.4:c.436G>C