Canonical Allele Identifier: PA645412717
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 228179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile34527Thr
CA1985583
NM_001267550.2:c.103580T>C