Canonical Allele Identifier: PA280649
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97540
ClinVar Variation Id: 97541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ser242Arg
CA280647
NM_000243.3:c.726C>A
CA280650
NM_000243.3:c.726C>G
CA394478123
NM_000243.3:c.724A>C