Canonical Allele Identifier: PA658667535
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr28493Ala
CA60984661
NM_001267550.2:c.85477A>G