Canonical Allele Identifier: PA2829445851
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1469597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser26287Pro
CA60953469
NM_003319.4:c.78859T>C