Allele Registry

Canonical Allele Identifier: PA916011531

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000009496

ClinVar Variation:

89379

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Cys999_Val1000delinsLeu	CA012733 NM_001281492.2:c.2996_2998del