Canonical Allele Identifier: PA2830236310
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg16471Trp
CA1989963
NM_133437.4:c.49411C>T