Canonical Allele Identifier: PA2825099791
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1209626
ClinVar RCV Id: RCV001578714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Pro306Ser
CA276899102
NM_000243.3:c.916C>T