Allele Registry

Canonical Allele Identifier: PA2826624915

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000476123

RCV000562563

RCV000587170

RCV001824790

RCV003463941

RCV004001853

ClinVar Variation:

410512

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg118Pro	CA073426 NM_001281492.2:c.353G>C