Canonical Allele Identifier: PA2827617603
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 155743
ClinVar RCV Id: RCV000143814 RCV000794428 RCV002408640 RCV004544322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Glu623Asp
CA233093
NM_001351528.2:c.1869A>C
CA375338145
NM_001351528.2:c.1869A>T