Canonical Allele Identifier: PA2825971477
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 459624
ClinVar RCV Id: RCV000548549 RCV003139758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Asn27Ser
CA6311917
NM_001164278.2:c.80A>G