Canonical Allele Identifier: PA2829446339
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val26799Ala
CA302948
NM_003319.4:c.80396T>C