Canonical Allele Identifier: PA2825615235
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_001120959.1:p.Val2578Gly
CA369220119
NM_001127487.2:c.7733T>G