Allele Registry

Canonical Allele Identifier: PA2825088835

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003182637

ClinVar Variation:

2453182

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser616_Leu617insPro	CA2580067713 NM_000179.3:c.1847_1849dup