Canonical Allele Identifier: PA2825963748
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Arg374Trp
CA116970
NM_001163812.2:c.1120C>T