Canonical Allele Identifier: PA108918
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 426104
ClinVar RCV Id: RCV000508722
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Gln458His
CA378210724
NM_021830.4:c.1374G>C
CA378210725
NM_021830.4:c.1374G>T