Canonical Allele Identifier: PA645411042
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg25344Trp
CA1989963
NM_001267550.2:c.76030C>T