Allele Registry

Canonical Allele Identifier: PA2826630176

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003078884

ClinVar Variation:

2162051

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu161Lys	CA346745060 NM_001281493.2:c.481G>A