Canonical Allele Identifier: PA2829446108
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Leu26561Val
CA181557
NM_003319.4:c.79681T>G