Canonical Allele Identifier: PA915983039
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 646885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp591Asn
CA4474471
NM_001458.5:c.1771G>A