Canonical Allele Identifier: PA645412961
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val35928Glu
CA1984876
NM_001267550.2:c.107783T>A