Canonical Allele Identifier: PA2826489380
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 393026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1425Val
CA2005349
NM_001267550.2:c.4274C>T