Allele Registry

Canonical Allele Identifier: PA2826464971

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001524677

ClinVar Variation:

1171495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asp594Val	CA346728866 NM_001258281.1:c.1781A>T