Canonical Allele Identifier: PA2825976841
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21285
ClinVar RCV Id: RCV000020448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Val1592Asp
CA341847
NM_001164319.2:c.4775T>A