Canonical Allele Identifier: PA141192
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47497
ClinVar RCV Id: RCV000040766 RCV000082444 RCV000269727 RCV000320246 RCV000364179 RCV000310741 RCV000365525 RCV000617583 RCV000852796 RCV001083905 RCV001798194
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg30179His
CA141188
NM_001267550.2:c.90536G>A