Canonical Allele Identifier: PA2825963578
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 214181
ClinVar RCV Id: RCV000195756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Cys113Ser
CA320131
NM_001163812.2:c.338G>C
CA378206944
NM_001163812.2:c.337T>A