Allele Registry

Canonical Allele Identifier: PA915963905

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 648188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser445Arg	CA346744540 NM_000179.3:c.1333A>C CA346744554 NM_000179.3:c.1335T>A CA346744555 NM_000179.3:c.1335T>G