Allele Registry

Canonical Allele Identifier: PA135989

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.0732969469

Score -0.107069984

Score -0.1648312377

Score -0.1786684538

Linked Data - NCBI & NCI

ClinVar Allele:

54471

ClinVar RCV:

RCV000038464

RCV000548489

RCV000681055

RCV001030071

RCV002257383

RCV003421952

RCV004018874

ClinVar Variation:

45304

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly138Ser	CA135988 NM_005343.4:c.412G>A