Canonical Allele Identifier: PA2827261615
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_001315557.1:p.Leu432Phe
CA340067666
NM_001328628.1:c.1294C>T