Canonical Allele Identifier: PA2826221806
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 495752
ClinVar RCV Id: RCV000587448 RCV001829616 RCV002476273 RCV003126833 RCV003126832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185465.2:p.Val330Ala
CA276896167
NM_001198536.2:c.989T>C