Canonical Allele Identifier: PA2830219263
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met15121Thr
CA140649
NM_133432.3:c.45362T>C