Canonical Allele Identifier: PA280291
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 36516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val33Leu
CA280289
NM_000243.3:c.97G>T
CA394484780
NM_000243.3:c.97G>C