Canonical Allele Identifier: PA915985612
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 553652
ClinVar RCV Id: RCV000669148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Tyr296Asp
CA229597269
NM_001467.6:c.886T>G