Canonical Allele Identifier: PA2825963817
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1802980
ClinVar RCV Id: RCV003233001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Trp474Ser
CA212963554
NM_001163812.2:c.1421G>C