Canonical Allele Identifier: PA2580122103
Gene: SLC6A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2210082
ClinVar RCV Id: RCV002686714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003841.1:p.Phe253Ser
CA3182855
NM_001003841.3:c.758T>C