Canonical Allele Identifier: PA2825971949
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551501
ClinVar RCV Id: RCV000666579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Phe7Leu
CA382905737
NM_001164279.2:c.21C>G
CA382905738
NM_001164279.2:c.21C>A
CA382905747
NM_001164279.2:c.19T>C