Canonical Allele Identifier: PA2825851959
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 650071
ClinVar RCV Id: RCV000805153 RCV001830746 RCV002534802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Ala30Val
CA10549150
NM_001142805.2:c.89C>T