Canonical Allele Identifier: PA658664688
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp4766Asn
CA60982481
NM_001267550.2:c.14296G>A