Canonical Allele Identifier: PA645381583
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 378132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val487Leu
CA7860122
NM_000243.3:c.1459G>C
CA394464204
NM_000243.3:c.1459G>T