Canonical Allele Identifier: PA658810135
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 533700
ClinVar RCV Id: RCV000640931 RCV001255373 RCV002251491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Pro382Leu
CA415086073
NM_005629.4:c.1145C>T