Canonical Allele Identifier: PA2829446472
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile26921Thr
CA16610284
NM_003319.4:c.80762T>C