Canonical Allele Identifier: PA139490
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46909
ClinVar RCV Id: RCV000040179 RCV000172679 RCV000247302 RCV000769039 RCV001081699 RCV001133178 RCV001133179 RCV001132263 RCV001132265 RCV001132264 RCV004534895
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val11622Ile
CA139486
NM_001267550.2:c.34864G>A