Allele Registry

Canonical Allele Identifier: PA2826627627

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000529411

RCV000581939

RCV001000818

RCV003459169

RCV004003681

RCV004546513

ClinVar Variation:

455213

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys755Glu	CA346755166 NM_001281492.2:c.2263A>G