Canonical Allele Identifier: PA2826221821
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 3230735
ClinVar RCV Id: RCV004522850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Thr338Ile
CA394458829
NM_001198536.2:c.1013C>T