Canonical Allele Identifier: PA2826221722
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.His267Tyr
CA115610
NM_001198536.2:c.799C>T