Canonical Allele Identifier: PA2827261778
Gene: SLC6A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613343
ClinVar RCV Id: RCV003362292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001315558.1:p.Leu497Phe
CA340067666
NM_001328629.1:c.1489C>T