Canonical Allele Identifier: PA2741813784
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2637664
ClinVar RCV Id: RCV003404962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val726Asp
CA7859858
NM_000243.3:c.2177T>A