Canonical Allele Identifier: PA2830195465
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser13378Pro
CA309899
NM_133378.4:c.40132T>C