Canonical Allele Identifier: PA2829438693
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg16279Trp
CA1989963
NM_003319.4:c.48835C>T