Canonical Allele Identifier: PA2829440014
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg18463Trp
CA310671
NM_003319.4:c.55387C>T