Canonical Allele Identifier: PA280663
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala268Val
CA280661
NM_000243.3:c.803C>T