Canonical Allele Identifier: PA915988195
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68279
ClinVar RCV Id: RCV000059130 RCV001390447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Ala75Val
CA219316
NM_001164279.2:c.224C>T