Canonical Allele Identifier: PA645409383
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu9352Ser
CA1999665
NM_001267550.2:c.28055T>C