Canonical Allele Identifier: PA2829430141
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala1339Thr
CA181990
NM_003319.4:c.4015G>A