Canonical Allele Identifier: PA645382686
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Leu1000Phe
CA2005669
NM_133379.5:c.2998C>T