Canonical Allele Identifier: PA2825963900
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 694438
ClinVar RCV Id: RCV000855769 RCV002536207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157285.1:p.Trp20Cys
CA212963556
NM_001163813.2:c.60G>T
CA378210872
NM_001163813.2:c.60G>C