Allele Registry

Canonical Allele Identifier: PA2826636990

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218455

RCV000467310

ClinVar Variation:

232917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu693Lys	CA10578125 NM_001281494.2:c.2077G>A