Canonical Allele Identifier: PA2825972633
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2979970
ClinVar RCV Id: RCV003835080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Asp200Tyr
CA382901964
NM_001164280.2:c.598G>T