Allele Registry

Canonical Allele Identifier: PA2825092052

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 638837

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr1225Lys	CA071830 NM_000179.3:c.3674C>A