Canonical Allele Identifier: PA915978576
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 660972
ClinVar RCV Id: RCV000818285 RCV003437438 RCV004028950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Glu50Lys
CA10454378
NM_006517.5:c.148G>A