Canonical Allele Identifier: PA2825613268
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472073
ClinVar RCV Id: RCV000531313 RCV000788621 RCV002330945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1543Trp
CA4475405
NM_001127487.2:c.4627C>T