Canonical Allele Identifier: PA111754
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 492806
ClinVar RCV Id: RCV000582702 RCV002530823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008927.1:p.Ser143Phe
CA1233071
NM_006996.3:c.428C>T