Canonical Allele Identifier: PA2830199058
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile21872Thr
CA1990381
NM_133378.4:c.65615T>C