Canonical Allele Identifier: PA280675
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97550
ClinVar RCV Id: RCV000083802 RCV000594000 RCV002262656 RCV003114248 RCV003126494 RCV003126493 RCV002483165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala289Val
CA280673
NM_000243.3:c.866C>T