Canonical Allele Identifier: PA2825975359
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1685823
ClinVar RCV Id: RCV002249990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Pro1603Ser
CA353352205
NM_001164318.2:c.4807C>T