Allele Registry

Canonical Allele Identifier: PA2826465860

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV004522954

ClinVar Variation:

3230840

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln813Glu	CA346731314 NM_001258281.1:c.2437C>G