Canonical Allele Identifier: PA2829441157
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile20306Thr
CA1988198
NM_003319.4:c.60917T>C