Canonical Allele Identifier: PA1139704402
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 848238
ClinVar RCV Id: RCV001051950 RCV002355036 RCV003396672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1999Trp
CA4475847
NM_001458.5:c.5995C>T