Canonical Allele Identifier: PA2826221830
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1386886
ClinVar RCV Id: RCV001881680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Gln344Pro
CA394458551
NM_001198536.2:c.1031A>C