Canonical Allele Identifier: PA645376066
Gene: SLC6A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319797
ClinVar RCV Id: RCV000887054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165975.1:p.Thr283Arg
CA8061582
NM_001172504.1:c.848C>G