Canonical Allele Identifier: PA2829438423
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr15790Ile
CA310496
NM_003319.4:c.47369C>T