Canonical Allele Identifier: PA2826174669
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Ala246Val
CA280392
NM_001198536.2:c.737C>T