Allele Registry

Canonical Allele Identifier: PA2826630625

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001012840

RCV001050588

RCV004004518

ClinVar Variation:

819904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile268Met	CA346748569 NM_001281493.2:c.804A>G