Canonical Allele Identifier: PA658809457
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp6935His
CA309902
NM_003319.4:c.20803G>C