Canonical Allele Identifier: PA2825852757
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1285397
ClinVar RCV Id: RCV001706753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Leu297Pro
CA415086592
NM_001142806.1:c.890T>C