Canonical Allele Identifier: PA2826221741
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 378132
ClinVar RCV Id: RCV000439116 RCV000531412 RCV001712195 RCV002263676 RCV003150813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Val276Leu
CA7860122
NM_001198536.2:c.826G>C
CA394464204
NM_001198536.2:c.826G>T