Canonical Allele Identifier: PA916065700
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val6921Ile
CA184456
NM_133437.4:c.20761G>A