Allele Registry

Canonical Allele Identifier: PA2826463009

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000233177

RCV000410808

RCV000565216

RCV000590509

RCV001251062

RCV002478486

RCV003483528

RCV003998484

ClinVar Variation:

182583

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala123Gly	CA021433 NM_001258281.1:c.368C>G