Canonical Allele Identifier: PA222961
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95421
ClinVar RCV Id: RCV001251643 RCV003905062 RCV000514434 RCV001087210 RCV001847654 RCV002362728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Gln138Glu
CA222960
NM_006517.5:c.412C>G