Canonical Allele Identifier: PA916066293
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile8034Val
CA309977
NM_133437.4:c.24100A>G