Canonical Allele Identifier: PA1139702624
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 939234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp820Asn
CA166175565
NM_001458.5:c.2458G>A