Canonical Allele Identifier: PA2826221839
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 864685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.His350Tyr
CA276896126
NM_001198536.2:c.1048C>T