Canonical Allele Identifier: PA2829431968
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val4455Leu
CA231595
NM_003319.4:c.13363G>C