Canonical Allele Identifier: PA645411787
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala29110Val
CA1988331
NM_001267550.2:c.87329C>T