Canonical Allele Identifier: PA2829443018
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala23031Thr
CA141378
NM_003319.4:c.69091G>A