Canonical Allele Identifier: PA280516
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Lys695Asn
CA280514
NM_000243.3:c.2085G>C
CA394486080
NM_000243.3:c.2085G>T