Canonical Allele Identifier: PA2829432488
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg5461Gln
CA139665
NM_003319.4:c.16382G>A