Canonical Allele Identifier: PA658665421
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 457998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro633Leu
CA276955244
NM_000243.3:c.1898C>T