Canonical Allele Identifier: PA283319
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47016
ClinVar RCV Id: RCV000040286 RCV000227469 RCV000337139 RCV000285222 RCV000342472 RCV000302752 RCV000391758 RCV000621575 RCV000769005 RCV001085025
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu15913Phe
CA283315
NM_001267550.2:c.47737C>T