Allele Registry

Canonical Allele Identifier: PA2825091867

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001020663

RCV002551829

ClinVar Variation:

823958

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser1195Arg	CA346760518 NM_000179.3:c.3583A>C CA346760523 NM_000179.3:c.3585T>A CA346760524 NM_000179.3:c.3585T>G