Allele Registry

Canonical Allele Identifier: PA108869

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV000004884

ClinVar Variation:

4621

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Arg354Pro	CA116963 NM_021830.4:c.1061G>C