Canonical Allele Identifier: PA2573185955
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1523107
ClinVar RCV Id: RCV002036515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Asp1629Asn
CA2468866
NM_001164317.2:c.4885G>A