Canonical Allele Identifier: PA2825963574
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1514850
ClinVar RCV Id: RCV002029602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Thr97Ser
CA5653048
NM_001163812.2:c.290C>G
CA378206688
NM_001163812.2:c.289A>T