Allele Registry

Canonical Allele Identifier: PA2826174580

Gene: MEFV HGNC NCBI

ClinVar Variation Id: 279848

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185465.2:p.Ala100Val	CA7860272 NM_001198536.2:c.299C>T