Canonical Allele Identifier: PA2825971239
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 666169
ClinVar RCV Id: RCV000824605 RCV002487862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Arg197His
CA229598954
NM_001164277.2:c.590G>A