Allele Registry

Canonical Allele Identifier: PA2826626495

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002413091

ClinVar Variation:

1781404

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu489Gly	CA346749772 NM_001281492.2:c.1466A>G