Canonical Allele Identifier: PA2826221855
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Met371Leu
CA280431
NM_001198536.2:c.1111A>C
CA394490445
NM_001198536.2:c.1111A>T