Allele Registry

Canonical Allele Identifier: PA108849

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV001581548

ClinVar Variation:

1210826

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Arg303Trp	CA378208813 NM_021830.4:c.907C>T