Canonical Allele Identifier: PA2580112378
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2177038
ClinVar RCV Id: RCV002585337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Trp547Arg
CA276896157
NM_000243.3:c.1639T>C
CA394458899
NM_000243.3:c.1639T>A