Canonical Allele Identifier: PA2830216446
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala10463Pro
CA1992894
NM_133432.3:c.31387G>C