ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825972042
Gene: SLC37A4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002900408
ClinVar Variation:
2045000
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001157751.1:p.Arg124Cys
CA6311806
NM_001164279.2:c.370C>T