Allele Registry

Canonical Allele Identifier: PA169108

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000076370

RCV000132039

RCV000202225

RCV000524373

RCV001264415

RCV001588897

RCV003452883

RCV003455975

ClinVar Variation:

90868

2673350

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly683Arg	CA019900 NM_000251.3:c.2047G>A CA346729142 NM_000251.3:c.2047G>C