Canonical Allele Identifier: PA2825973465
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 284104
ClinVar RCV Id: RCV000314947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Asn164Lys
CA10604687
NM_001164317.2:c.492C>G
CA353333548
NM_001164317.2:c.492C>A