Canonical Allele Identifier: PA1139702925
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 807837
ClinVar RCV Id: RCV000996039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Lys19del
CA915952140
NM_005629.4:c.55_57del