Canonical Allele Identifier: PA658665411
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 457996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ser503Cys
CA7860112
NM_000243.3:c.1508C>G