Allele Registry

Canonical Allele Identifier: PA658749767

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 490008

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe1222Leu	CA346760838 NM_000179.3:c.3664T>C CA346760843 NM_000179.3:c.3666T>A CA346760844 NM_000179.3:c.3666T>G