Canonical Allele Identifier: PA658815230
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala21856Thr
CA1991684
NM_001267550.2:c.65566G>A