Allele Registry

Canonical Allele Identifier: PA2826626285

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398914

ClinVar Variation:

1778575

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly441Cys	CA346748576 NM_001281492.2:c.1321G>T