Allele Registry

Canonical Allele Identifier: PA916010889

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000490967

RCV000549468

RCV000759128

RCV003464056

RCV004003459

RCV004535548

ClinVar Variation:

428380

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr6Pro	CA068021 NM_001281492.2:c.16A>C