Allele Registry

Canonical Allele Identifier: PA2826634001

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491543

RCV001856944

RCV004003464

ClinVar Variation:

428408

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu1020Val	CA072394 NM_001281493.2:c.3059A>T