Allele Registry

Canonical Allele Identifier: PA2826624861

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001239065

RCV004034595

ClinVar Variation:

964772

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln106Glu	CA346739981 NM_001281492.2:c.316C>G