Canonical Allele Identifier: PA116971
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 4629
ClinVar RCV Id: RCV000004892 RCV000523637
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Arg374Trp
CA116970
NM_021830.4:c.1120C>T