Allele Registry

Canonical Allele Identifier: PA2826628071

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000223636

RCV000465720

RCV000589846

RCV000708883

RCV003462404

ClinVar Variation:

229716

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg858Leu	CA069886 NM_001281492.2:c.2573G>T