Canonical Allele Identifier: PA2825976006
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2083254
ClinVar RCV Id: RCV003002390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Gly172Val
CA353333601
NM_001164319.2:c.515G>T