Canonical Allele Identifier: PA2826221682
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 319113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Val258Ala
CA7860134
NM_001198536.2:c.773T>C