Canonical Allele Identifier: PA2826429002
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33724Asp
CA1985166
NM_001256850.1:c.101171G>A