Canonical Allele Identifier: PA2825099646
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 2689420
ClinVar RCV Id: RCV003488025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro50Ala
CA394484252
NM_000243.3:c.148C>G