Canonical Allele Identifier: PA2829332307
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 3221706
ClinVar RCV Id: RCV004511030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gln613Pro
CA369227179
NM_001458.5:c.1838A>C