Canonical Allele Identifier: PA302470
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser15884Pro
CA302469
NM_133378.4:c.47650T>C