Canonical Allele Identifier: PA2830207705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val8363Met
CA1999513
NM_133378.4:c.25087G>A