Canonical Allele Identifier: PA2825975349
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21285
ClinVar RCV Id: RCV000020448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Val1592Asp
CA341847
NM_001164318.2:c.4775T>A