Canonical Allele Identifier: PA093566
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97508
ClinVar RCV Id: RCV000083760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro758Ser
CA280564
NM_000243.3:c.2272C>T