Canonical Allele Identifier: PA2826174585
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 36514
ClinVar Variation Id: 426837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Arg103His
CA280283
NM_001198536.2:c.308G>A
CA645294087
NM_001198536.2:c.308_309delinsAT