Allele Registry

Canonical Allele Identifier: PA108770

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV000020866

RCV002251876

ClinVar Variation:

4630

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Ala318Thr	CA342356 NM_021830.4:c.952G>A