Allele Registry

Canonical Allele Identifier: PA2826635704

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 89248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Cys392Arg	CA009656 NM_001281494.2:c.1174T>C