Canonical Allele Identifier: PA658814122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala15018Glu
CA1995514
NM_001267550.2:c.45053C>A