Canonical Allele Identifier: PA2580112116
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2311078
ClinVar RCV Id: RCV002896639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ser108Thr
CA394482456
NM_000243.3:c.323G>C