Canonical Allele Identifier: PA2826174617
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Arg137His
CA280361
NM_001198536.2:c.410G>A