Canonical Allele Identifier: PA2830210784
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 393026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala1379Val
CA2005349
NM_133432.3:c.4136C>T