Canonical Allele Identifier: PA916061082
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val9478Ile
CA1998714
NM_133378.4:c.28432G>A