Canonical Allele Identifier: PA2829434832
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr9707Ala
CA16610408
NM_003319.4:c.29119A>G