Canonical Allele Identifier: PA2829445872
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1761050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr26305Ala
CA60953427
NM_003319.4:c.78913A>G