Canonical Allele Identifier: PA2826174693
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97448
ClinVar Variation Id: 2697902
ClinVar RCV Id: RCV003498154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Arg290His
CA280412
NM_001198536.2:c.869G>A
CA2697549665
NM_001198536.2:c.869_870delinsAT