Canonical Allele Identifier: PA2573217902
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1402606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro2556Ala
CA4476336
NM_001458.5:c.7666C>G