Canonical Allele Identifier: PA891850091
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 576043
ClinVar RCV Id: RCV000698439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2151Cys
CA369212571
NM_001458.5:c.6451G>T