Canonical Allele Identifier: PA2825613147
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1011402
ClinVar RCV Id: RCV001309192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp1495Asn
CA4475356
NM_001127487.2:c.4483G>A