Allele Registry

Canonical Allele Identifier: PA2826635157

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398914

ClinVar Variation:

1778575

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly269Cys	CA346748576 NM_001281494.2:c.805G>T