Canonical Allele Identifier: PA2830235248
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr14651Ala
CA310409
NM_133437.4:c.43951A>G