Canonical Allele Identifier: PA2826221852
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 369971
ClinVar RCV Id: RCV000408827 RCV001269727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Thr366Asn
CA10654935
NM_001198536.2:c.1097C>A