Canonical Allele Identifier: PA2580544486
Gene: SLC51B HGNC NCBI
ClinVar RCV:
RCV002852505
ClinVar Variation:
2022466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Ala7Val
CA392870491
NM_178859.4:c.20C>T