Canonical Allele Identifier: PA645470613
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 372367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Gly530Trp
CA2467856
NM_001457.4:c.1588G>T