Allele Registry

Canonical Allele Identifier: PA2826464685

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000542666

RCV002404371

RCV003459178

ClinVar Variation:

455524

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu529Phe	CA346728296 NM_001258281.1:c.1585C>T