Canonical Allele Identifier: PA2825972811
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555634
ClinVar RCV Id: RCV000671492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Tyr343Cys
CA382896151
NM_001164280.2:c.1028A>G