Canonical Allele Identifier: PA2825615161
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2930197
ClinVar RCV Id: RCV003787555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Leu2517Pro
CA369219513
NM_001127487.2:c.7550T>C