Canonical Allele Identifier: PA2826221492
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1385298
ClinVar RCV Id: RCV001871326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Gly114Arg
CA276899006
NM_001198536.2:c.340G>C