Canonical Allele Identifier: PA2825852297
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503222
ClinVar RCV Id: RCV002022714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Asp406Gly
CA415086626
NM_001142805.2:c.1217A>G