Canonical Allele Identifier: PA2580168978
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2441475
ClinVar RCV Id: RCV003144016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Phe2557Tyr
CA2469726
NM_001164317.2:c.7670T>A