Canonical Allele Identifier: PA658808804
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro1102Ser
CA4475013
NM_001458.5:c.3304C>T