Canonical Allele Identifier: PA658666282
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr20856Cys
CA1992209
NM_001267550.2:c.62567A>G