Canonical Allele Identifier: PA2829437896
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Trp14880Arg
CA1990582
NM_003319.4:c.44638T>C
CA349650430
NM_003319.4:c.44638T>A