Canonical Allele Identifier: PA645412562
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr33350Ile
CA1986085
NM_001267550.2:c.100049C>T