Canonical Allele Identifier: PA658665368
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 450323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Arg178Trp
CA394480937
NM_000243.3:c.532C>T