Allele Registry

Canonical Allele Identifier: PA645470961

Gene: MSH2 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -4.8129358572

Linked Data - NCBI & NCI

ClinVar Allele:

392830

405748

ClinVar RCV:

RCV000456279

RCV000485060

RCV000552453

RCV000572631

RCV001025005

RCV003150218

ClinVar Variation:

408469

419807

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg21Leu	CA16610840 NM_000251.3:c.62_63delinsTT CA16617546 NM_000251.3:c.62G>T