Allele Registry

Canonical Allele Identifier: PA2499230050

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001323282

RCV002447369

ClinVar Variation:

1023266

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Cys778Trp	CA346729924 NM_000251.3:c.2334C>G