Canonical Allele Identifier: PA2829330146
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1006578
ClinVar RCV Id: RCV001303641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Ile1590Thr
CA353352128
NM_001457.4:c.4769T>C