Allele Registry

Canonical Allele Identifier: PA2826634293

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 410445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr21Ile	CA073667 NM_001281494.2:c.62C>T