Canonical Allele Identifier: PA2826174643
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 450568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Asp180Asn
CA7860224
NM_001198536.2:c.538G>A