Allele Registry

Canonical Allele Identifier: PA2573164905

Gene: MEFV HGNC NCBI

ClinVar RCV:

RCV001965702

ClinVar Variation:

1461131

HGVS (amino-acid)	Matching Registered Transcripts
NP_000234.1:p.Thr577Ile	CA394490501 NM_000243.3:c.1730C>T