Canonical Allele Identifier: PA645412774
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser34855Tyr
CA10613205
NM_001267550.2:c.104564C>A