Canonical Allele Identifier: PA2825615213
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2441516
ClinVar RCV Id: RCV003144057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2560Ile
CA369219982
NM_001127487.2:c.7679C>T