Canonical Allele Identifier: PA2825615193
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1303834
ClinVar RCV Id: RCV001758127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Leu2539His
CA369219802
NM_001127487.2:c.7616T>A