Canonical Allele Identifier: PA2580262774
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1751206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.His2013Gln
CA369211017
NM_001458.5:c.6039C>A
CA369211019
NM_001458.5:c.6039C>G