Canonical Allele Identifier: PA1139675021
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 886836
ClinVar RCV Id: RCV001119245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ser749Tyr
CA7859847
NM_000243.3:c.2246C>A