Allele Registry

Canonical Allele Identifier: PA2826627788

Gene: MSH6 HGNC NCBI

ClinVar Allele:

393088

ClinVar RCV:

RCV000460470

RCV002255396

RCV003470465

ClinVar Variation:

410467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu789Asp	CA16611013 NM_001281492.2:c.2367A>C CA346755433 NM_001281492.2:c.2367A>T