Canonical Allele Identifier: PA915988262
Gene: FLNB HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ala1674Ser
CA341851
NM_001164317.2:c.5020G>T