Canonical Allele Identifier: PA915966562
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 646446
ClinVar RCV Id: RCV000800729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Gly776Ala
CA394484285
NM_000243.3:c.2327G>C