Canonical Allele Identifier: PA645409461
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala10095Thr
CA1999195
NM_001267550.2:c.30283G>A