Canonical Allele Identifier: PA2499258155
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1020737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro1490Ser
CA4475353
NM_001458.5:c.4468C>T