Canonical Allele Identifier: PA2826221828
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1717409
ClinVar RCV Id: RCV002304770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Gln340Glu
CA394458790
NM_001198536.2:c.1018C>G