Canonical Allele Identifier: PA2825614285
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1379445
ClinVar RCV Id: RCV001883778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Leu2018Arg
CA369211441
NM_001127487.2:c.6053T>G