Allele Registry

Canonical Allele Identifier: PA2573061950

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001763145

RCV004040161

ClinVar Variation:

1307609

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly759Arg	CA346729809 NM_000251.3:c.2275G>A CA346729810 NM_000251.3:c.2275G>C