Canonical Allele Identifier: PA2829435160
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala10338Pro
CA1992894
NM_003319.4:c.31012G>C