Canonical Allele Identifier: PA645411253
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr27053Asn
CA1989244
NM_001267550.2:c.81157T>A