Allele Registry

Canonical Allele Identifier: PA2826625820

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000477991

RCV000564326

RCV000815191

ClinVar Variation:

418323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe331Cys	CA16617651 NM_001281492.2:c.992T>G