Canonical Allele Identifier: PA2580544498
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 2129034
ClinVar RCV Id: RCV003040341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Lys100Glu
CA392842761
NM_178859.4:c.298A>G