Allele Registry

Canonical Allele Identifier: PA2825090138

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002760424

ClinVar Variation:

1970543

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln939Glu	CA346755643 NM_000179.3:c.2815C>G