Canonical Allele Identifier: PA2825963891
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 426105
ClinVar RCV Id: RCV000508820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157285.1:p.Leu10Pro
CA378210783
NM_001163813.2:c.29T>C