Canonical Allele Identifier: PA2573164889
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 1463761
ClinVar RCV Id: RCV001997785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000234.1:p.Thr249Ser
CA394477935
NM_000243.3:c.745A>T
CA2573152020
NM_000243.3:c.744_745delinsCT