Allele Registry

Canonical Allele Identifier: PA2826464854

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000547904

RCV000568306

RCV001572130

RCV002481753

RCV004003740

ClinVar Variation:

455532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg565Lys	CA346728562 NM_001258281.1:c.1694G>A