Canonical Allele Identifier: PA2825975779
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1417463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Arg2335Cys
CA2469592
NM_001164318.2:c.7003C>T