Canonical Allele Identifier: PA280683
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97554
ClinVar RCV Id: RCV000083806 RCV000214115 RCV001719850 RCV002262657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Thr309Met
CA280681
NM_000243.3:c.926C>T