Canonical Allele Identifier: PA2827616762
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365353
ClinVar RCV Id: RCV000348389 RCV000400900 RCV000644810 RCV002338959 RCV003482252 RCV004544710
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Arg1538Trp
CA5297167
NM_001351527.2:c.4612C>T