Canonical Allele Identifier: PA2825615151
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 3236021
ClinVar RCV Id: RCV004555282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp2510His
CA369219415
NM_001127487.2:c.7528G>C