Allele Registry

Canonical Allele Identifier: PA645383012

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218181

RCV000458194

RCV000491101

RCV000623975

RCV002467444

RCV003165582

RCV003463615

ClinVar Variation:

234622

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Tyr969Cys	CA069803 NM_000179.3:c.2906A>G