Canonical Allele Identifier: PA2741884599
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2946775
ClinVar RCV Id: RCV003809013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly1115Cys
CA369196560
NM_001458.5:c.3343G>T