Canonical Allele Identifier: PA093481
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2539
ClinVar RCV Id: RCV000002648 RCV000220431 RCV000589706 RCV000763380 RCV002262540 RCV004528066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Met694Ile
CA027824
NM_000243.3:c.[2082G>A;442G>C]
CA280093
NM_000243.3:c.2082G>A
CA394486098
NM_000243.3:c.2082G>C
CA394486111
NM_000243.3:c.2082G>T