Canonical Allele Identifier: PA2825972190
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Met242Val
CA6311684
NM_001164279.2:c.724A>G