Canonical Allele Identifier: PA280427
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97453
ClinVar RCV Id: RCV000083705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Leu559Phe
CA280425
NM_000243.3:c.1675C>T