Allele Registry

Canonical Allele Identifier: PA2826632445

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000219717

RCV000792117

RCV003463593

RCV003998583

ClinVar Variation:

233859

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu690Gly	CA10578124 NM_001281493.2:c.2069A>G