Canonical Allele Identifier: PA2829442171
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp21863His
CA141274
NM_003319.4:c.65587G>C