Allele Registry

Canonical Allele Identifier: PA2826630833

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003182637

ClinVar Variation:

2453182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ser314_Leu315insPro	CA2580067713 NM_001281493.2:c.941_943dup