Canonical Allele Identifier: PA2825971829
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3032086
ClinVar RCV Id: RCV003899820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly292Ala
CA382898187
NM_001164278.2:c.875G>C