Canonical Allele Identifier: PA2829439715
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Tyr17988Asn
CA1989244
NM_003319.4:c.53962T>A