Canonical Allele Identifier: PA645412870
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr35490His
CA1985100
NM_001267550.2:c.106468T>C