Canonical Allele Identifier: PA658678551
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 452999
ClinVar RCV Id: RCV000522249 RCV000705455 RCV002329244 RCV003486857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1474Trp
CA4475327
NM_001458.5:c.4420C>T