Canonical Allele Identifier: PA2825975370
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1490901
ClinVar RCV Id: RCV001986135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Gly1612Ser
CA353352252
NM_001164318.2:c.4834G>A