Canonical Allele Identifier: PA658659206
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His35480Arg
CA60953022
NM_001267550.2:c.106439A>G