Canonical Allele Identifier: PA2830190979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 393026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala1425Val
CA2005349
NM_133378.4:c.4274C>T