Canonical Allele Identifier: PA2826032803
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338256
ClinVar RCV Id: RCV001817627 RCV003772337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Pro197Ser
CA1011404
NM_001166496.2:c.589C>T