Allele Registry

Canonical Allele Identifier: PA2826221848

Gene: MEFV HGNC NCBI

ClinVar RCV:

RCV001965702

ClinVar Variation:

1461131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185465.2:p.Thr366Ile	CA394490501 NM_001198536.2:c.1097C>T