Canonical Allele Identifier: PA2829434421
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg9000Cys
CA310055
NM_003319.4:c.26998C>T