Canonical Allele Identifier: PA2829436492
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404624
ClinVar RCV Id: RCV000477442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile12626Thr
CA16610321
NM_003319.4:c.37877T>C