Canonical Allele Identifier: PA1139705231
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 860247
ClinVar RCV Id: RCV001066522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ile2707Met
CA369221917
NM_001458.5:c.8121T>G