Canonical Allele Identifier: PA108957
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4622

Amino-acid Alleles

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