Canonical Allele Identifier: PA110350
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21463
ClinVar RCV Id: RCV000020651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Ser120Phe
CA342116
NM_006517.5:c.359C>T