Canonical Allele Identifier: PA140508
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
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro20476Ser
CA140506
NM_133378.4:c.61426C>T