Canonical Allele Identifier: PA2580171927
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2114201
ClinVar RCV Id: RCV003042668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Ser434Ile
CA394488997
NM_001198536.2:c.1301G>T