Allele Registry

Canonical Allele Identifier: PA2825089718

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 2752948

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser823Arg	CA346754103 NM_000179.3:c.2467A>C CA346754113 NM_000179.3:c.2469T>A CA346754115 NM_000179.3:c.2469T>G