Canonical Allele Identifier: PA2825963631
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2100712
ClinVar RCV Id: RCV003014539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Trp208_Phe209insSerSerProGly
CA2580081109
NM_001163812.2:c.625_626insCCTCCCCTGGGT