Canonical Allele Identifier: PA645410010
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro16453Thr
CA1994613
NM_001267550.2:c.49357C>A