Canonical Allele Identifier: PA179193
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro3303Leu
CA179191
NM_001267550.2:c.9908C>T