Canonical Allele Identifier: PA658832739
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 556291
ClinVar RCV Id: RCV000672284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Ala170Thr
CA382902708
NM_001164277.2:c.508G>A