Allele Registry

Canonical Allele Identifier: PA2826465867

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001889948

ClinVar Variation:

1377625

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly814Ala	CA346731331 NM_001258281.1:c.2441G>C