Canonical Allele Identifier: PA2825963892
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1344247
ClinVar RCV Id: RCV001848350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157285.1:p.Glu11Asp
CA378210795
NM_001163813.2:c.33A>C
CA378210797
NM_001163813.2:c.33A>T