Allele Registry

Canonical Allele Identifier: PA2826221849

Gene: MEFV HGNC NCBI

ClinVar RCV:

RCV000083707

RCV000989481

ClinVar Variation:

97455

803186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185465.2:p.Thr366Ser	CA280429 NM_001198536.2:c.1096A>T CA394490502 NM_001198536.2:c.1097C>G