Canonical Allele Identifier: PA280369
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Arg354Trp
CA280367
NM_000243.3:c.1060C>T