Canonical Allele Identifier: PA2830205096
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr300Asn
CA2006201
NM_133378.4:c.899C>A