Canonical Allele Identifier: PA2829440764
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1163426
ClinVar RCV Id: RCV001508467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val19701Leu
CA349544887
NM_003319.4:c.59101G>C