Allele Registry

Canonical Allele Identifier: PA109047

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV000004887

ClinVar Variation:

4624

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Ser369Tyr	CA116967 NM_021830.4:c.1106C>A