Canonical Allele Identifier: PA658809372
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr4534Ile
CA309755
NM_003319.4:c.13601C>T