Canonical Allele Identifier: PA2825613034
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2938150
ClinVar RCV Id: RCV003796972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val1440Met
CA369201161
NM_001127487.2:c.4318G>A