Canonical Allele Identifier: PA2825976846
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21286
ClinVar RCV Id: RCV000020449
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Ser1602Pro
CA341848
NM_001164319.2:c.4804T>C