Canonical Allele Identifier: PA915988251
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21285
ClinVar RCV Id: RCV000020448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Val1623Asp
CA341847
NM_001164317.2:c.4868T>A