Canonical Allele Identifier: PA280579
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala89Thr
CA280577
NM_000243.3:c.265G>A