Canonical Allele Identifier: PA2825973853
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 3095659
ClinVar RCV Id: RCV004389457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ala850Val
CA353345670
NM_001164317.2:c.2549C>T