Canonical Allele Identifier: PA2580262508
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2133982
ClinVar RCV Id: RCV003064177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly605Ala
CA369227132
NM_001458.5:c.1814G>C