Canonical Allele Identifier: PA093692
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val726Ala
CA280095
NM_000243.3:c.2177T>C