Canonical Allele Identifier: PA341130
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 11698
ClinVar RCV Id: RCV000012464 RCV000483506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Phe408del
CA341129
NM_005629.4:c.1222_1224del