Canonical Allele Identifier: PA2830193547
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser7993Ala
CA312121
NM_133378.4:c.23977T>G