Canonical Allele Identifier: PA099870
Gene: SLC27A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 5746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005085.2:p.Gln300Arg
CA117716
NM_005094.4:c.899A>G