Canonical Allele Identifier: PA658816175
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp27496Asn
CA1989062
NM_001267550.2:c.82486G>A