Canonical Allele Identifier: PA645382547
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val871Leu
CA2005776
NM_133379.5:c.2611G>T
CA349496292
NM_133379.5:c.2611G>C