Canonical Allele Identifier: PA2830218611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47265
ClinVar RCV Id: RCV000040535 RCV000242208 RCV000270511 RCV000275015 RCV000366186 RCV000325543 RCV000360261 RCV000488277 RCV000769965 RCV000852818 RCV001079297 RCV001293210 RCV003993767 RCV002222367
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro14104Ser
CA140506
NM_133432.3:c.42310C>T