Canonical Allele Identifier: PA1139739276
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 872774
ClinVar RCV Id: RCV001093423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Pro83Leu
CA378206489
NM_021830.4:c.248C>T