Canonical Allele Identifier: PA2826221494
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97556
ClinVar RCV Id: RCV000083808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Val117Ala
CA280686
NM_001198536.2:c.350T>C