Canonical Allele Identifier: PA093229
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Arg408Gln
CA280116
NM_000243.3:c.1223G>A