Canonical Allele Identifier: PA2825612340
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 954190
ClinVar RCV Id: RCV001226606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro1126Arg
CA369196666
NM_001127487.2:c.3377C>G