Allele Registry

Canonical Allele Identifier: PA645470882

Gene: MSH2 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -5.0165627384

Linked Data - NCBI & NCI

ClinVar Allele:

238802

ClinVar RCV:

RCV000227770

RCV000480195

RCV000563870

RCV002465579

RCV003469135

RCV003998750

ClinVar Variation:

237357

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln4Lys	CA10581987 NM_000251.3:c.10C>A