Canonical Allele Identifier: PA2825611127
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2133982
ClinVar RCV Id: RCV003064177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly605Ala
CA369227132
NM_001127487.2:c.1814G>C