Allele Registry

Canonical Allele Identifier: PA2826463928

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000132166

RCV000212599

RCV000411777

RCV000765665

RCV000781558

RCV001083003

RCV001356152

RCV001798264

ClinVar Variation:

90569

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg340Gln	CA017527 NM_001258281.1:c.1019G>A