Allele Registry

Canonical Allele Identifier: PA331644

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076650

RCV001854333

RCV003315405

RCV004019518

ClinVar Variation:

91146

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Cys199Arg	CA021524 NM_000251.3:c.595T>C