Canonical Allele Identifier: PA645411913
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu29912Pro
CA1987875
NM_001267550.2:c.89735T>C