Canonical Allele Identifier: PA2830219257
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg15116Ser
CA10611620
NM_133432.3:c.45346C>A