Canonical Allele Identifier: PA2580544496
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 1978177
ClinVar RCV Id: RCV002741702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.His86Gln
CA7613512
NM_178859.4:c.258C>G
CA392842575
NM_178859.4:c.258C>A