Canonical Allele Identifier: PA325442
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 214172
ClinVar RCV Id: RCV000200862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Met114Leu
CA325441
NM_021830.4:c.340A>T
CA378206952
NM_021830.4:c.340A>C