Canonical Allele Identifier: PA183903
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg9365Gln
CA183901
NM_001267550.2:c.28094G>A