Canonical Allele Identifier: PA2825974897
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 3095659
ClinVar RCV Id: RCV004389457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Ala850Val
CA353345670
NM_001164318.2:c.2549C>T