Allele Registry

Canonical Allele Identifier: PA2826631339

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000483131

RCV000571852

RCV001238127

RCV004003395

ClinVar Variation:

423126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg430Pro	CA16617670 NM_001281493.2:c.1289G>C