Canonical Allele Identifier: PA645412191
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 228169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val31717Ile
CA1986999
NM_001267550.2:c.95149G>A