Allele Registry

Canonical Allele Identifier: PA2826464115

Gene: MSH2 HGNC NCBI

ClinVar Allele:

150578

ClinVar RCV:

RCV000129078

RCV000210120

RCV000482497

RCV000524342

RCV000662718

RCV000781551

ClinVar Variation:

140864

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys383Asn	CA018049 NM_001258281.1:c.1149G>C CA346724703 NM_001258281.1:c.1149G>T