Allele Registry

Canonical Allele Identifier: PA2826628630

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001372799

ClinVar Variation:

1063009

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu1066Lys	CA46717430 NM_001281492.2:c.3196G>A