Canonical Allele Identifier: PA2825975107
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 346334
ClinVar RCV Id: RCV000349068 RCV000915285 RCV002502330 RCV002278561
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Val1195Met
CA2468451
NM_001164318.2:c.3583G>A