Canonical Allele Identifier: PA341852
Gene: FLNB HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Ala1643Ser
CA341851
NM_001457.4:c.4927G>T