Canonical Allele Identifier: PA2741929091
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2501493
ClinVar RCV Id: RCV003227288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Pro65Ala
CA413655969
NM_006517.5:c.193C>G