Canonical Allele Identifier: PA2825964047
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2768494
ClinVar RCV Id: RCV003576409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157286.1:p.Lys16Thr
CA378210839
NM_001163814.2:c.47A>C