Canonical Allele Identifier: PA302632
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly13352Glu
CA302630
NM_001256850.1:c.40055G>A