Canonical Allele Identifier: PA2826174771
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Arg440Cys
CA280438
NM_001198536.2:c.1318C>T