Canonical Allele Identifier: PA658678485
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly885Arg
CA4474815
NM_001458.5:c.2653G>A
CA369192784
NM_001458.5:c.2653G>C