Canonical Allele Identifier: PA916060077
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 694435
ClinVar RCV Id: RCV000855766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Arg192Cys
CA378207697
NM_021830.4:c.574C>T