Canonical Allele Identifier: PA645408861
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala4846Thr
CA2002382
NM_001267550.2:c.14536G>A