Canonical Allele Identifier: PA645409870
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 288762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile15254Phe
CA1995375
NM_001267550.2:c.45760A>T