Canonical Allele Identifier: PA109047
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4624
ClinVar RCV Id: RCV000004887
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Ser369Tyr
CA116967
NM_021830.4:c.1106C>A