Canonical Allele Identifier: PA280660
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ile259Val
CA280658
NM_000243.3:c.775A>G