Allele Registry

Canonical Allele Identifier: PA345393

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076204

RCV000410514

RCV000491263

RCV000524349

RCV000588411

RCV001175346

ClinVar Variation:

90707

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg534Cys	CA018706 NM_000251.3:c.1600C>T