Allele Registry

Canonical Allele Identifier: PA094676

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000001829

RCV000076197

RCV000165648

RCV000256140

RCV000531855

RCV001251063

ClinVar Variation:

1759

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg524Pro	CA018643 NM_000251.3:c.1571G>C