Canonical Allele Identifier: PA184057
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179252
ClinVar RCV Id: RCV000156039 RCV001128995 RCV001131670 RCV001131667 RCV001131668 RCV001131669
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr7053Pro
CA184055
NM_001267550.2:c.21157A>C