Canonical Allele Identifier: PA2741924197
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2661708
ClinVar RCV Id: RCV003432589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Leu401Ile
CA10549448
NM_005629.4:c.1201C>A