Canonical Allele Identifier: PA235581
Gene: SLC27A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 156263
ClinVar RCV Id: RCV000162310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005085.2:p.Arg275Cys
CA235580
NM_005094.4:c.823C>T