Canonical Allele Identifier: PA2825963652
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1940022
ClinVar RCV Id: RCV002658198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.His245Tyr
CA378208285
NM_001163812.2:c.733C>T