Allele Registry

Canonical Allele Identifier: PA2826625076

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000807815

RCV004028631

ClinVar Variation:

652286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu156Gln	CA346740574 NM_001281492.2:c.466G>C