Canonical Allele Identifier: PA108849
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1210826
ClinVar RCV Id: RCV001581548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Arg303Trp
CA378208813
NM_021830.4:c.907C>T