Canonical Allele Identifier: PA2829432622
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1328881
ClinVar RCV Id: RCV001797513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.His5691Pro
CA349645187
NM_003319.4:c.17072A>C