Canonical Allele Identifier: PA2830213356
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp4901Asn
CA302489
NM_133432.3:c.14701G>A