Canonical Allele Identifier: PA280394
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala457Val
CA280392
NM_000243.3:c.1370C>T