Canonical Allele Identifier: PA2826489372
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1384Ser
CA2005396
NM_001267550.2:c.4150G>T