Canonical Allele Identifier: PA2826428493
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33214Tyr
CA10613205
NM_001256850.1:c.99641C>A