Canonical Allele Identifier: PA248450
Gene: SLC6A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 208186
ClinVar RCV Id: RCV000190382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003841.1:p.Cys49Tyr
CA248449
NM_001003841.3:c.146G>A