Allele Registry

Canonical Allele Identifier: PA2826628109

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218455

RCV000467310

ClinVar Variation:

232917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu865Lys	CA10578125 NM_001281492.2:c.2593G>A