Canonical Allele Identifier: PA2826429107
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.His33839Arg
CA60953022
NM_001256850.1:c.101516A>G