Canonical Allele Identifier: PA2499258067
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1014929
ClinVar RCV Id: RCV001313732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly1898Asp
CA369208034
NM_001458.5:c.5693G>A