Canonical Allele Identifier: PA2829445061
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg25572Trp
CA311160
NM_003319.4:c.76714C>T