Allele Registry

Canonical Allele Identifier: PA2826626487

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003182637

ClinVar Variation:

2453182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser486_Leu487insPro	CA2580067713 NM_001281492.2:c.1457_1459dup