Allele Registry

Canonical Allele Identifier: PA2826464822

Gene: MSH2 HGNC NCBI

ClinVar Allele:

16792

ClinVar RCV:

RCV000001823

RCV000076307

RCV000566777

RCV000630204

RCV002460877

ClinVar Variation:

1753

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro556Leu	CA019478 NM_001258281.1:c.1667C>T