Canonical Allele Identifier: PA658814374
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile17059Val
CA1994231
NM_001267550.2:c.51175A>G