Allele Registry

Canonical Allele Identifier: PA2826465864

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV004014351

ClinVar Variation:

3074817

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln813His	CA346731321 NM_001258281.1:c.2439A>C CA346731322 NM_001258281.1:c.2439A>T