Canonical Allele Identifier: PA108783
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4618
ClinVar RCV Id: RCV000004881 RCV000508874 RCV002512779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Ala359Thr
CA116959
NM_021830.4:c.1075G>A