Canonical Allele Identifier: PA108839
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Arg303Gln
CA116969
NM_021830.4:c.908G>A