Canonical Allele Identifier: PA2825615178
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 549664
ClinVar RCV Id: RCV000714272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Tyr2530Cys
CA369219679
NM_001127487.2:c.7589A>G