Canonical Allele Identifier: PA2830243122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr26144Ala
CA311205
NM_133437.4:c.78430A>G