Canonical Allele Identifier: PA1139674359
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 849552
ClinVar RCV Id: RCV001053548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Cys332Tyr
CA394471368
NM_000243.3:c.995G>A