Canonical Allele Identifier: PA2825611605
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2946490
ClinVar RCV Id: RCV003808728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp820Glu
CA4474738
NM_001127487.2:c.2460C>A
CA369191666
NM_001127487.2:c.2460C>G