Canonical Allele Identifier: PA2741884736
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2632681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ser2182Gly
CA369212787
NM_001458.5:c.6544A>G