Canonical Allele Identifier: PA645410345
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala19403Pro
CA1992894
NM_001267550.2:c.58207G>C