Canonical Allele Identifier: PA142039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47849
ClinVar RCV Id: RCV000041118 RCV000462754 RCV001088266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile3641Thr
CA142036
NM_001267550.2:c.10922T>C