Canonical Allele Identifier: PA2825615173
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1402606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro2523Ala
CA4476336
NM_001127487.2:c.7567C>G