Canonical Allele Identifier: PA2825974720
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 372367
ClinVar RCV Id: RCV000412741 RCV002480263 RCV002523908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Gly530Trp
CA2467856
NM_001164318.2:c.1588G>T