Canonical Allele Identifier: PA2573217814
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1369853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ser1927Gly
CA166189044
NM_001458.5:c.5779A>G