Canonical Allele Identifier: PA915966466
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 647727
ClinVar RCV Id: RCV000802293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro228Ser
CA394478486
NM_000243.3:c.682C>T