Canonical Allele Identifier: PA2825974792
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2314330
ClinVar RCV Id: RCV002905270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Asn664Ser
CA353342228
NM_001164318.2:c.1991A>G