Canonical Allele Identifier: PA280688
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97556
ClinVar RCV Id: RCV000083808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val328Ala
CA280686
NM_000243.3:c.983T>C