Canonical Allele Identifier: PA311093
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala33316Thr
CA311091
NM_001267550.2:c.99946G>A