Canonical Allele Identifier: PA2580112207
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1694345
ClinVar RCV Id: RCV002262067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala207Ser
CA394479033
NM_000243.3:c.619G>T