Canonical Allele Identifier: PA2825975351
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1197292
ClinVar RCV Id: RCV001561063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Val1592Ile
CA2468861
NM_001164318.2:c.4774G>A