Canonical Allele Identifier: PA2825613181
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2185342
ClinVar RCV Id: RCV002603769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr1509Ala
CA4475367
NM_001127487.2:c.4525A>G