Canonical Allele Identifier: PA096532
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21285
ClinVar RCV Id: RCV000020448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Val1592Asp
CA341847
NM_001457.4:c.4775T>A