Canonical Allele Identifier: PA141122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47473
ClinVar RCV Id: RCV000040742 RCV000270510 RCV000327903 RCV000362829 RCV000384731 RCV000334082 RCV000618175 RCV000475243 RCV000725444 RCV001798192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly29364Ser
CA141118
NM_001267550.2:c.88090G>A