Canonical Allele Identifier: PA2829431677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Cys3934Gly
CA179026
NM_003319.4:c.11800T>G