Canonical Allele Identifier: PA139190
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_596869.4:p.Asn7647Ser
CA139188
NM_133378.4:c.22940A>G