Canonical Allele Identifier: PA2825974799
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 346317
ClinVar RCV Id: RCV000294860 RCV001850837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Pro679Ser
CA2467997
NM_001164318.2:c.2035C>T