Canonical Allele Identifier: PA2830212621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala3506Pro
CA2004068
NM_133432.3:c.10516G>C