Canonical Allele Identifier: PA2741884706
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2942621
ClinVar RCV Id: RCV003807787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val1896Gly
CA369208007
NM_001458.5:c.5687T>G