Allele Registry

Canonical Allele Identifier: PA094683

Gene: MSH2 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -3.11600145

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000030253

RCV000035361

RCV000144619

RCV000162398

RCV000757470

RCV001353586

RCV002490419

RCV003149584

ClinVar Variation:

36577

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn127Ser	CA021092 NM_000251.3:c.380A>G CA3054204375 NM_000251.3:c.380_384delinsGTCTT