Canonical Allele Identifier: PA280898
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 160359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Arg361Thr
CA280896
NM_000243.3:c.1082G>C