Canonical Allele Identifier: PA2499229956
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1009611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ser107Ala
CA7860457
NM_000243.3:c.319T>G