Canonical Allele Identifier: PA2825611804
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 854139
ClinVar RCV Id: RCV001059112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp903Asn
CA369192972
NM_001127487.2:c.2707G>A