Allele Registry

Canonical Allele Identifier: PA2826635361

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003182637

ClinVar Variation:

2453182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser314_Leu315insPro	CA2580067713 NM_001281494.2:c.941_943dup