Canonical Allele Identifier: PA1139669084
Gene: SLC6A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 973486
ClinVar RCV Id: RCV001250112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003841.1:p.Leu238Phe
CA359067536
NM_001003841.3:c.712C>T