Canonical Allele Identifier: PA2830205753
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val28791Ile
CA310935
NM_133378.4:c.86371G>A