Allele Registry

Canonical Allele Identifier: PA2826631936

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164528

RCV000205577

RCV000662485

RCV001580460

RCV002271437

RCV003462138

ClinVar Variation:

185159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Met573Thr	CA010617 NM_001281493.2:c.1718T>C