Canonical Allele Identifier: PA2825611224
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 660655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp646Asn
CA4474535
NM_001127487.2:c.1936G>A