Canonical Allele Identifier: PA2499229961
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1011684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ser159Gly
CA276902835
NM_000243.3:c.475A>G