Canonical Allele Identifier: PA2825974497
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1307396
ClinVar RCV Id: RCV001760814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Ile153Asn
CA353333470
NM_001164318.2:c.458T>A