Canonical Allele Identifier: PA2830216711
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro10922Leu
CA283515
NM_133432.3:c.32765C>T