Canonical Allele Identifier: PA2830205979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1329220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val29003Met
CA60972536
NM_133378.4:c.87007G>A