Canonical Allele Identifier: PA2829438577
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile16056Val
CA310511
NM_003319.4:c.48166A>G