Canonical Allele Identifier: PA2829430113
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu1313Gly
CA302567
NM_003319.4:c.3938A>G