Canonical Allele Identifier: PA2830233258
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro11398Thr
CA10613278
NM_133437.4:c.34192C>A