Canonical Allele Identifier: PA2826174649
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 457994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Arg197Trp
CA7860213
NM_001198536.2:c.589C>T