Allele Registry

Canonical Allele Identifier: PA2825090022

Gene: MSH6 HGNC NCBI

ClinVar Allele:

2731133

ClinVar RCV:

RCV003278532

ClinVar Variation:

2567491

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu905Ser	CA346755343 NM_000179.3:c.2714T>C