Allele Registry

Canonical Allele Identifier: PA915963539

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000807815

RCV004028631

ClinVar Variation:

652286

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu286Gln	CA346740574 NM_000179.3:c.856G>C