Canonical Allele Identifier: PA2829443858
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala24251Thr
CA311091
NM_003319.4:c.72751G>A