Canonical Allele Identifier: PA645510071
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 439738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Arg36His
CA2467454
NM_001457.4:c.107G>A