Canonical Allele Identifier: PA2829442795
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly22726Asp
CA358832
NM_003319.4:c.68177G>A