Canonical Allele Identifier: PA2825976858
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2663010
ClinVar RCV Id: RCV003441675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Gly1612Arg
CA353352251
NM_001164319.2:c.4834G>C