Canonical Allele Identifier: PA915988201
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551890
ClinVar RCV Id: RCV000667054 RCV003278980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Leu78Pro
CA382903424
NM_001164279.2:c.233T>C