Allele Registry

Canonical Allele Identifier: PA108957

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV000004885

RCV000508905

ClinVar Variation:

4622

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Leu381Pro	CA116964 NM_021830.4:c.1142T>C