Canonical Allele Identifier: PA280549
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97502
ClinVar RCV Id: RCV000083754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Phe743Tyr
CA280547
NM_000243.3:c.2228T>A