Canonical Allele Identifier: PA2827617223
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 155748
ClinVar RCV Id: RCV000143819 RCV000302102 RCV000393538 RCV000251546 RCV001080640 RCV001260210 RCV001847770
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Ile2547Thr
CA233108
NM_001351527.2:c.7640T>C