Canonical Allele Identifier: PA658665035
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu8005Gln
CA2000516
NM_001267550.2:c.24013G>C