Canonical Allele Identifier: PA302907
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val20798Ala
CA302906
NM_133378.4:c.62393T>C