Canonical Allele Identifier: PA2825611873
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2585961
ClinVar RCV Id: RCV003358181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val935Leu
CA369193310
NM_001127487.2:c.2803G>C