Canonical Allele Identifier: PA2580177000
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1926779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu34790Pro
CA349411890
NM_001267550.2:c.104369T>C