Canonical Allele Identifier: PA2825611828
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2951409
ClinVar RCV Id: RCV003805111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly912Asp
CA369193081
NM_001127487.2:c.2735G>A