Canonical Allele Identifier: PA2826221817
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2177038
ClinVar RCV Id: RCV002585337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Trp336Arg
CA276896157
NM_001198536.2:c.1006T>C
CA394458899
NM_001198536.2:c.1006T>A