Canonical Allele Identifier: PA1139674238
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 940448
ClinVar RCV Id: RCV001210039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala268Asp
CA7860324
NM_000243.3:c.803C>A