Allele Registry

Canonical Allele Identifier: PA2826632577

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000227649

RCV000491202

RCV000985838

RCV002494619

RCV003998725

ClinVar Variation:

237175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg722Trp	CA10582076 NM_001281493.2:c.2164C>T