Canonical Allele Identifier: PA2580346621
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2162992
ClinVar RCV Id: RCV003070527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Glu66Gly
CA413655977
NM_006517.5:c.197A>G