Allele Registry

Canonical Allele Identifier: PA2826464872

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV003165204

ClinVar Variation:

2447350

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala570Thr	CA346728614 NM_001258281.1:c.1708G>A