Canonical Allele Identifier: PA891863137
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 591331
ClinVar RCV Id: RCV000722509 RCV002535033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Ala139Ser
CA7860431
NM_000243.3:c.415G>T
CA891862990
NM_000243.3:c.414_415delinsGT