Canonical Allele Identifier: PA658815488
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala23389Gly
CA349664518
NM_001267550.2:c.70166C>G