Canonical Allele Identifier: PA2826221547
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Pro158Ser
CA280114
NM_001198536.2:c.472C>T