Canonical Allele Identifier: PA108869
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4621
ClinVar RCV Id: RCV000004884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Arg354Pro
CA116963
NM_021830.4:c.1061G>C