Canonical Allele Identifier: PA280397
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Val469Leu
CA280395
NM_000243.3:c.1405G>T
CA394464758
NM_000243.3:c.1405G>C