Canonical Allele Identifier: PA645410248
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val18479Ile
CA1993445
NM_001267550.2:c.55435G>A