Canonical Allele Identifier: PA2826174612
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1004030
ClinVar RCV Id: RCV001300667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Gln132His
CA394470948
NM_001198536.2:c.396G>T
CA394470951
NM_001198536.2:c.396G>C