Canonical Allele Identifier: PA2830213018
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val4302Met
CA311746
NM_133432.3:c.12904G>A