Allele Registry

Canonical Allele Identifier: PA645381671

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000483131

RCV000571852

RCV001238127

RCV004003395

ClinVar Variation:

423126

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg732Pro	CA16617670 NM_000179.3:c.2195G>C