Canonical Allele Identifier: PA238232
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val2930Ile
CA238228
NM_133379.5:c.8788G>A