Canonical Allele Identifier: PA645412858
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35367Met
CA1985165
NM_001267550.2:c.106100C>T