Canonical Allele Identifier: PA645383070
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 393026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala1425Val
CA2005349
NM_133379.5:c.4274C>T