Canonical Allele Identifier: PA2573061911
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1321574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala768Gly
CA7859838
NM_000243.3:c.2303C>G