Canonical Allele Identifier: PA645381098
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 392469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Glu163Asp
CA7860418
NM_000243.3:c.489G>T
CA394481210
NM_000243.3:c.489G>C