Canonical Allele Identifier: PA2826221536
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Pro153Leu
CA280373
NM_001198536.2:c.458C>T