Canonical Allele Identifier: PA2826032820
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3067437
ClinVar RCV Id: RCV003993126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Gly235Arg
CA1011382
NM_001166496.2:c.703G>C
CA341828404
NM_001166496.2:c.703G>A