Canonical Allele Identifier: PA174919
Gene: SLC6A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 161857
ClinVar RCV Id: RCV000149393 RCV002516004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_964012.2:p.Glu266Lys
CA174918
NM_201649.4:c.796G>A