Canonical Allele Identifier: PA1139674761
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 918000
ClinVar RCV Id: RCV001175245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val543Leu
CA394459039
NM_000243.3:c.1627G>C