Canonical Allele Identifier: PA658666902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly24506Asp
CA1990358
NM_001267550.2:c.73517G>A