Canonical Allele Identifier: PA658806313
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala1384Ser
CA2005396
NM_133379.5:c.4150G>T