Canonical Allele Identifier: PA207835
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu35910Lys
CA207833
NM_001267550.2:c.107728G>A