Canonical Allele Identifier: PA2830195681
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro13885Thr
CA1994613
NM_133378.4:c.41653C>A