Allele Registry

Canonical Allele Identifier: PA2825976004

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020452

ClinVar Variation:

38344

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Leu171Gln	CA341853 NM_001164319.2:c.512T>A