Canonical Allele Identifier: PA2825963639
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2091186
ClinVar RCV Id: RCV003013482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Cys226Phe
CA212962920
NM_001163812.2:c.677G>T