Allele Registry

Canonical Allele Identifier: PA2499229325

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001349078

ClinVar Variation:

1044775

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu493Ala	CA346746013 NM_000179.3:c.1478A>C