Canonical Allele Identifier: PA2827616636
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2142203
ClinVar RCV Id: RCV003058944 RCV003076256 RCV003234220 RCV003234219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Tyr1297Phe
CA5297310
NM_001351527.2:c.3890A>T