Canonical Allele Identifier: PA2829335260
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551256
ClinVar RCV Id: RCV000666264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Trp330Ser
CA6311643
NM_001467.6:c.989G>C