Canonical Allele Identifier: PA1139687250
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 951731
ClinVar RCV Id: RCV001223713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Asp97Tyr
CA7860275
NM_001198536.2:c.289G>T