Canonical Allele Identifier: PA2825099611
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2102387
ClinVar RCV Id: RCV003037680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Thr4Ala
CA394486932
NM_000243.3:c.10A>G