Canonical Allele Identifier: PA645412362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile32508Met
CA1986530
NM_001267550.2:c.97524A>G