Canonical Allele Identifier: PA309078
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val22373Asp
CA309076
NM_001267550.2:c.67118T>A