Canonical Allele Identifier: PA2826221760
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 457996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Ser292Cys
CA7860112
NM_001198536.2:c.875C>G