Canonical Allele Identifier: PA2826221811
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 918000
ClinVar RCV Id: RCV001175245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Val332Leu
CA394459039
NM_001198536.2:c.994G>C