Canonical Allele Identifier: PA2826174588
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2130436
ClinVar RCV Id: RCV003052077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Cys104Arg
CA394471904
NM_001198536.2:c.310T>C