Canonical Allele Identifier: PA645381553
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 319113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val469Ala
CA7860134
NM_000243.3:c.1406T>C