Allele Registry

Canonical Allele Identifier: PA2826626272

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000629901

RCV002404726

ClinVar Variation:

525697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe439Leu	CA346748540 NM_001281492.2:c.1315T>C CA346748550 NM_001281492.2:c.1317C>A CA346748554 NM_001281492.2:c.1317C>G