Allele Registry

Canonical Allele Identifier: PA108889

Gene: TWNK HGNC NCBI

ClinVar RCV:

RCV000508920

RCV000517894

RCV000626956

ClinVar Variation:

426106

HGVS (amino-acid)	Matching Registered Transcripts
NP_068602.2:p.Arg374Gln	CA378209878 NM_021830.4:c.1121G>A