Allele Registry

Canonical Allele Identifier: PA2826636417

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 859835

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly562Arg	CA346754849 NM_001281494.2:c.1684G>C CA346754859 NM_001281494.2:c.1684G>A