Canonical Allele Identifier: PA658728681
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 495752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val541Ala
CA276896167
NM_000243.3:c.1622T>C