Canonical Allele Identifier: PA2830219822
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Trp16113Ser
CA1990091
NM_133432.3:c.48338G>C