Canonical Allele Identifier: PA2829438560
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala16022Thr
CA1990080
NM_003319.4:c.48064G>A