Canonical Allele Identifier: PA658810136
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 523485
ClinVar RCV Id: RCV000626885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Ala403Val
CA415086472
NM_005629.4:c.1208C>T