Canonical Allele Identifier: PA2499258118
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1024816
ClinVar RCV Id: RCV001325043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro653Leu
CA369227450
NM_001458.5:c.1958C>T