Canonical Allele Identifier: PA139192
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46785
ClinVar RCV Id: RCV000040055 RCV000284411 RCV000289133 RCV000327811 RCV000333598 RCV000381135 RCV000488131 RCV001084221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn8891Ser
CA139188
NM_001267550.2:c.26672A>G