Canonical Allele Identifier: PA2825971371
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2074546
ClinVar RCV Id: RCV002976289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Pro358Ser
CA6311634
NM_001164277.2:c.1072C>T