Allele Registry

Canonical Allele Identifier: PA2826462824

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001960257

ClinVar Variation:

1442394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu27Val	CA346729584 NM_001258281.1:c.79C>G