Canonical Allele Identifier: PA302633
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly14993Glu
CA302630
NM_001267550.2:c.44978G>A