Canonical Allele Identifier: PA140885
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47398
ClinVar RCV Id: RCV000040668 RCV000620281 RCV000768913 RCV001086543 RCV000461664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile25539Thr
CA140882
NM_001256850.1:c.76616T>C