Allele Registry

Canonical Allele Identifier: PA2826634827

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000776440

RCV002230121

RCV002508935

RCV003446065

ClinVar Variation:

410487

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ala192Ser	CA067740 NM_001281494.2:c.574G>T