Allele Registry

Canonical Allele Identifier: PA093650

Gene: MEFV HGNC NCBI

ClinVar RCV:

RCV000083707

RCV000989481

ClinVar Variation:

97455

803186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000234.1:p.Thr577Ser	CA280429 NM_000243.3:c.1729A>T CA394490502 NM_000243.3:c.1730C>G