Canonical Allele Identifier: PA2828287812
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1344247
ClinVar RCV Id: RCV001848350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355204.1:p.Glu11Asp
CA378210795
NM_001368275.1:c.33A>C
CA378210797
NM_001368275.1:c.33A>T