Canonical Allele Identifier: PA2580273436
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2075927
ClinVar RCV Id: RCV002979022 RCV002979023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003042.3:p.Thr352Ile
CA1011338
NM_003051.4:c.1055C>T