Canonical Allele Identifier: PA2499241869
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1063261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Tyr19Cys
CA7860547
NM_001198536.2:c.56A>G