Allele Registry

Canonical Allele Identifier: PA2826465407

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160609

RCV000218725

RCV000456427

RCV003453268

ClinVar Variation:

182578

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala697Val	CA020406 NM_001258281.1:c.2090C>T