Canonical Allele Identifier: PA2829439741
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly18036Val
CA310647
NM_003319.4:c.54107G>T