Canonical Allele Identifier: PA2742023435
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 2748522
ClinVar RCV Id: RCV003566022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Lys84Arg
CA392842545
NM_178859.4:c.251A>G