Allele Registry

Canonical Allele Identifier: PA2826635168

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001982099

RCV003289257

ClinVar Variation:

1432785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Phe271Leu	CA346748631 NM_001281494.2:c.811T>C CA346748664 NM_001281494.2:c.813T>A CA346748667 NM_001281494.2:c.813T>G