Canonical Allele Identifier: PA2830233317
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg11494Trp
CA183130
NM_133437.4:c.34480C>T