Canonical Allele Identifier: PA2825852319
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 588350
ClinVar RCV Id: RCV002314443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Leu423Phe
CA415086756
NM_001142805.2:c.1267C>T