Canonical Allele Identifier: PA272489
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 159901
ClinVar RCV Id: RCV000147493 RCV000415270 RCV001383614 RCV001267932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Gly327Arg
CA272488
NM_006517.5:c.979G>A
CA413657703
NM_006517.5:c.979G>C