Canonical Allele Identifier: PA658817157
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34188Lys
CA1985734
NM_001267550.2:c.102562G>A