Canonical Allele Identifier: PA2825613164
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2928668
ClinVar RCV Id: RCV003789442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1499Asp
CA369201886
NM_001127487.2:c.4496G>A