Canonical Allele Identifier: PA2741929088
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2730925
ClinVar RCV Id: RCV003588331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Pro51Ser
CA413655883
NM_006517.5:c.151C>T