Canonical Allele Identifier: PA916047249
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 56727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355204.1:p.Arg9Trp
CA264202
NM_001368275.1:c.25C>T