Canonical Allele Identifier: PA2825612449
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1366110
ClinVar RCV Id: RCV001961978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1168Cys
CA369197116
NM_001127487.2:c.3502G>T