Allele Registry

Canonical Allele Identifier: PA2826465573

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

50087

ClinVar RCV:

RCV000034556

RCV000121564

RCV000129519

RCV001030484

RCV001080801

RCV001093691

RCV001356651

RCV001787035

RCV004534720

ClinVar Variation:

41648

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu743Lys	CA020577 NM_001258281.1:c.2227G>A