Canonical Allele Identifier: PA2827616643
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2928318
ClinVar RCV Id: RCV003787140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Leu1310Phe
CA375327938
NM_001351527.2:c.3930A>T
CA375327939
NM_001351527.2:c.3930A>C