Canonical Allele Identifier: PA2825852289
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_001136277.1:p.Phe398del
CA341129
NM_001142805.2:c.1192_1194del