Canonical Allele Identifier: PA645380955
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 234472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Asn78Ser
CA7860501
NM_000243.3:c.233A>G