Canonical Allele Identifier: PA2825975382
Gene: FLNB HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Ala1643Ser
CA341851
NM_001164318.2:c.4927G>T