Canonical Allele Identifier: PA2825612410
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059644
ClinVar RCV Id: RCV001368973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro1155Ala
CA4475046
NM_001127487.2:c.3463C>G