Canonical Allele Identifier: PA645410539
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys21039Thr
CA10587487
NM_001267550.2:c.63116A>C