Canonical Allele Identifier: PA2830223582
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile22168Thr
CA1987318
NM_133432.3:c.66503T>C