Canonical Allele Identifier: PA658665395
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 457994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Arg408Trp
CA7860213
NM_000243.3:c.1222C>T