Canonical Allele Identifier: PA2825613122
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2450894
ClinVar RCV Id: RCV003177284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1486Ala
CA369201762
NM_001127487.2:c.4457G>C