Canonical Allele Identifier: PA342091
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 21448
ClinVar RCV Id: RCV000020635 RCV000623073 RCV000479265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Phe107del
CA342090
NM_005629.4:c.321_323del