Canonical Allele Identifier: PA2499258191
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1057285
ClinVar RCV Id: RCV001366235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2611Gly
CA369220119
NM_001458.5:c.7832T>G