Canonical Allele Identifier: PA129458
Gene: FFAR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 30774
ClinVar RCV Id: RCV000023753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_859529.2:p.Arg270His
CA129457
NM_181745.4:c.809G>A