Canonical Allele Identifier: PA2829438902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile16665Val
CA310560
NM_003319.4:c.49993A>G