Canonical Allele Identifier: PA2825852290
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 624450
ClinVar RCV Id: RCV000762678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Phe396Leu
CA415086524
NM_001142805.2:c.1186T>C
CA415086536
NM_001142805.2:c.1188C>A
CA415086537
NM_001142805.2:c.1188C>G