Canonical Allele Identifier: PA2825963569
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1345445
ClinVar RCV Id: RCV002037296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Gln89His
CA378206563
NM_001163812.2:c.267G>C
CA378206565
NM_001163812.2:c.267G>T