Canonical Allele Identifier: PA916060172
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 638300
ClinVar RCV Id: RCV000790907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Leu481Val
CA378210914
NM_021830.4:c.1441C>G