Canonical Allele Identifier: PA2825972550
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2910297
ClinVar RCV Id: RCV003619009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Trp138Arg
CA382903845
NM_001164280.2:c.412T>C
CA382903848
NM_001164280.2:c.412T>A