Canonical Allele Identifier: PA2826221819
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 633304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Thr337Asn
CA394458854
NM_001198536.2:c.1010C>A