Canonical Allele Identifier: PA2580112213
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1696110
ClinVar RCV Id: RCV002266254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro221Leu
CA394478669
NM_000243.3:c.662C>T