Canonical Allele Identifier: PA645412386
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32573Cys
CA1986502
NM_001267550.2:c.97717C>T