Allele Registry

Canonical Allele Identifier: PA2825090467

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003484586

RCV004364854

ClinVar Variation:

2683985

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1023Gln	CA346756538 NM_000179.3:c.3067G>C