Allele Registry

Canonical Allele Identifier: PA645472215

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001027097

RCV001358282

RCV002230810

RCV003470449

ClinVar Variation:

408531

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ser268Leu	CA040677 NM_000251.3:c.803C>T