Canonical Allele Identifier: PA2499258135
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 999407
ClinVar RCV Id: RCV001295403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Tyr926Asp
CA369193237
NM_001458.5:c.2776T>G