Canonical Allele Identifier: PA2825971873
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554872
ClinVar RCV Id: RCV000670580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Val320Leu
CA382897325
NM_001164278.2:c.958G>T
CA382897333
NM_001164278.2:c.958G>C