Canonical Allele Identifier: PA2825615189
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719320
ClinVar RCV Id: RCV002304933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro2535Leu
CA4476339
NM_001127487.2:c.7604C>T