Canonical Allele Identifier: PA916047247
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 806559
ClinVar RCV Id: RCV000994495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355204.1:p.Ala6Gly
CA378210745
NM_001368275.1:c.17C>G