Canonical Allele Identifier: PA2826210989
Gene: FFAR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 30774
ClinVar RCV Id: RCV000023753
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182684.1:p.Arg254His
CA129457
NM_001195755.2:c.761G>A