Canonical Allele Identifier: PA138894
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp6655Asn
CA138890
NM_001267550.2:c.19963G>A