Allele Registry

Canonical Allele Identifier: PA2826636875

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218181

RCV000458194

RCV000491101

RCV000623975

RCV002467444

RCV003165582

RCV003463615

ClinVar Variation:

234622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Tyr667Cys	CA069803 NM_001281494.2:c.2000A>G