Canonical Allele Identifier: PA2825963541
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 298494
ClinVar RCV Id: RCV000311980 RCV000350458 RCV000398995 RCV000406517 RCV001515622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Gly26Ser
CA5653019
NM_001163812.2:c.76G>A