Canonical Allele Identifier: PA2826278913
Gene: SLC19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 157588
ClinVar RCV Id: RCV000144916 RCV001788041 RCV002055868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192135.1:p.His27Arg
CA170984
NM_001205206.4:c.80A>G