Canonical Allele Identifier: PA2825972159
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555668
ClinVar RCV Id: RCV000671531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Asn222Ser
CA382898132
NM_001164279.2:c.665A>G