Canonical Allele Identifier: PA2825963609
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1449242
ClinVar RCV Id: RCV002004561 RCV004538676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Thr183Ser
CA5653082
NM_001163812.2:c.548C>G
CA378207611
NM_001163812.2:c.547A>T