Canonical Allele Identifier: PA2829432778
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala5953Glu
CA1995514
NM_003319.4:c.17858C>A