Canonical Allele Identifier: PA2829440407
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Tyr19085His
CA140988
NM_003319.4:c.57253T>C