Canonical Allele Identifier: PA280351
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 96982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro115Thr
CA280349
NM_000243.3:c.343C>A