Canonical Allele Identifier: PA2829430898
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala2560Thr
CA311490
NM_003319.4:c.7678G>A