Allele Registry

Canonical Allele Identifier: PA916011439

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115413

RCV000121585

RCV000204658

RCV000412360

RCV000586502

RCV001080360

RCV001798330

RCV003460816

ClinVar Variation:

127585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg965Cys	CA012434 NM_001281492.2:c.2893C>T