Canonical Allele Identifier: PA2830219707
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr15915Ile
CA310496
NM_133432.3:c.47744C>T