Canonical Allele Identifier: PA2826221725
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2545
ClinVar Variation Id: 2414425
ClinVar RCV Id: RCV003106758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Phe268Leu
CA280103
NM_001198536.2:c.804C>G
CA7860129
NM_001198536.2:c.804C>A
CA394464447
NM_001198536.2:c.802T>C
CA658760339
NM_001198536.2:c.[804C>G;277+1744G>C]