Canonical Allele Identifier: PA2826221782
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Ile302Thr
CA280418
NM_001198536.2:c.905T>C