Canonical Allele Identifier: PA2830207699
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr8334Met
CA312145
NM_133378.4:c.25001C>T