Canonical Allele Identifier: PA2829431668
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile3919Asn
CA2002659
NM_003319.4:c.11756T>A