Canonical Allele Identifier: PA2580544497
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 1975817
ClinVar RCV Id: RCV002755879 RCV004067860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Asn91Thr
CA7613517
NM_178859.4:c.272A>C