Canonical Allele Identifier: PA2829436748
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala13052Thr
CA184884
NM_003319.4:c.39154G>A