Canonical Allele Identifier: PA2829330156
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1333671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Ser1602Tyr
CA353352200
NM_001457.4:c.4805C>A