Canonical Allele Identifier: PA645396858
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 282064
ClinVar RCV Id: RCV000332634 RCV001279136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Leu293Pro
CA10604058
NM_001164277.2:c.878T>C