Canonical Allele Identifier: PA658816008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys26743Thr
CA1989375
NM_001267550.2:c.80228A>C