Canonical Allele Identifier: PA2829435699
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg11302Trp
CA183130
NM_003319.4:c.33904C>T