Canonical Allele Identifier: PA2830218790
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala14408Thr
CA237839
NM_133432.3:c.43222G>A