Canonical Allele Identifier: PA2573067317
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 493169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Ser441Thr
CA7859929
NM_001198536.2:c.1321T>A