Canonical Allele Identifier: PA2825963660
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2804656
ClinVar RCV Id: RCV003684201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Thr263Ser
CA378208462
NM_001163812.2:c.787A>T