Canonical Allele Identifier: PA916067086
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr9972Pro
CA1993236
NM_133437.4:c.29914A>C