Canonical Allele Identifier: PA2828287821
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4617
ClinVar RCV Id: RCV000004880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355204.1:p.Ala21Pro
CA116958
NM_001368275.1:c.61G>C