Canonical Allele Identifier: PA2826221787
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1804662
ClinVar RCV Id: RCV002469959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Lys308Met
CA394463322
NM_001198536.2:c.923A>T