Canonical Allele Identifier: PA2826032837
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1968163
ClinVar RCV Id: RCV002727294 RCV004548355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Leu267Val
CA341828190
NM_001166496.2:c.799C>G