Allele Registry

Canonical Allele Identifier: PA2826463650

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076002

RCV001213427

ClinVar Variation:

90507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu275Pro	CA016875 NM_001258281.1:c.824T>C