Canonical Allele Identifier: PA2825976834
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 591007
ClinVar RCV Id: RCV000722183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Arg1587Cys
CA353352105
NM_001164319.2:c.4759C>T