Canonical Allele Identifier: PA2825971718
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 139188
ClinVar RCV Id: RCV000128138 RCV000586546 RCV001083465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Asn198Ile
CA293573
NM_001164278.2:c.593A>T