Canonical Allele Identifier: PA2825613141
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 657016
ClinVar RCV Id: RCV000813558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1494Gln
CA369201854
NM_001127487.2:c.4481G>A