Canonical Allele Identifier: PA658806051
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr300Asn
CA2006201
NM_133379.5:c.899C>A