Canonical Allele Identifier: PA2829335308
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 841356
ClinVar RCV Id: RCV001043558 RCV002481906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Pro358Leu
CA6311633
NM_001467.6:c.1073C>T