Canonical Allele Identifier: PA2825613120
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1513438
ClinVar RCV Id: RCV002026172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1486Val
CA4475349
NM_001127487.2:c.4457G>T