Canonical Allele Identifier: PA2826221838
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97453
ClinVar RCV Id: RCV000083705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Leu348Phe
CA280425
NM_001198536.2:c.1042C>T