Canonical Allele Identifier: PA2825972177
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2143661
ClinVar RCV Id: RCV003062770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Met234Val
CA6311691
NM_001164279.2:c.700A>G