Allele Registry

Canonical Allele Identifier: PA108839

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV000004891

RCV001289123

ClinVar Variation:

4628

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Arg303Gln	CA116969 NM_021830.4:c.908G>A