Canonical Allele Identifier: PA2829445200
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala25686Pro
CA141656
NM_003319.4:c.77056G>C