Canonical Allele Identifier: PA2826221506
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1321575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Pro131Ser
CA276898954
NM_001198536.2:c.391C>T