Canonical Allele Identifier: PA645410869
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp23717Tyr
CA1990672
NM_001267550.2:c.71149G>T