Canonical Allele Identifier: PA1139674461
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 888171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro369Thr
CA7860232
NM_000243.3:c.1105C>A